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1 to 25 of 132  Show
  1. 1
    "Mouse Eya homologues of the Drosophila eyes absent gene require Pax6 for expression in lens and nasal placode."
    Xu P.-X., Woo I., Her H., Beier D.R., Maas R.L.
    Development 124:219-231(1997) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), TISSUE SPECIFICITY.
    Category: Expression, Sequences.
    Tissue: Embryo.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 35 other entries.

  2. 2
    "A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family."
    Abdelhak S., Kalatzis V., Heilig R., Compain S., Samson D., Vincent C., Weil D., Cruaud C., Sahly I., Leibovici M., Bitner-Glindzicz M., Francis M., Lacombe D., Vigneron J., Charachon R., Boven K., Bedbeder P., van Regemorter N., Weissenbach J., Petit C.
    Nat. Genet. 15:157-164(1997) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] (ISOFORM 2).
    Category: Sequences.
    Strain: CB/20.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3 and mapped to 11 other entries.

  3. 3
    Category: Sequences.
    Strain: C57BL/6J.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 40380 other entries.

  4. 4
    Mural R.J., Adams M.D., Myers E.W., Smith H.O., Venter J.C.
    Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  5. 5
    "Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome."
    Johnson K.R., Cook S.A., Erway L.C., Matthews A.N., Sanford L.P., Paradies N.E., Friedman R.A.
    Hum. Mol. Genet. 8:645-653(1999) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 276-321, DISEASE.
    Category: Pathology & Biotech, Sequences.
    Strain: 129/SvJ.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 8 other entries.

  6. 6
    Category: Sequences.
    Tissue: Embryo.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 9 and mapped to 8 other entries.

  7. 7
    "Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya."
    Ohto H., Kamada S., Tago K., Tominaga S., Ozaki H., Sato S., Kawakami K.
    Mol. Cell. Biol. 19:6815-6824(1999) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, INTERACTION WITH SIX2; SIX4 AND SIX5, SUBCELLULAR LOCATION.
    Category: Function, Subcellular Location, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 4 and mapped to 7 other entries.

  8. 8
    "Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia."
    Xu P.X., Adams J., Peters H., Brown M.C., Heaney S., Maas R.
    Nat. Genet. 23:113-117(1999) [PubMed] [Europe PMC] [Abstract]
    Cited for: DISRUPTION PHENOTYPE, FUNCTION.
    Category: Function, Pathology & Biotech.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 35 other entries.

  9. 9
    "Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis."
    Li X., Oghi K.A., Zhang J., Krones A., Bush K.T., Glass C.K., Nigam S.K., Aggarwal A.K., Maas R., Rose D.W., Rosenfeld M.G.
    Nature 426:247-254(2003) [PubMed] [Europe PMC] [Abstract]
    Cited for: FUNCTION, CATALYTIC ACTIVITY, DISRUPTION PHENOTYPE.
    Category: Function, Pathology & Biotech.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3 and mapped to 62 other entries.

  10. 10
    Cited for: CATALYTIC ACTIVITY.
    Category: Function.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3 and mapped to 19 other entries.

  11. 11
    "Pax6-dependence of Six3, Eya1 and Dach1 expression during lens and nasal placode induction."
    Purcell P., Oliver G., Mardon G., Donner A.L., Maas R.L.
    Gene Expr. Patterns 6:110-118(2005) [PubMed] [Europe PMC] [Abstract]
    Cited for: INTERACTION WITH SIX3.
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 33 other entries.

  12. 12
    "SUMO1 haploinsufficiency leads to cleft lip and palate."
    Alkuraya F.S., Saadi I., Lund J.J., Turbe-Doan A., Morton C.C., Maas R.L.
    Science 313:1751-1751(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: SUMOYLATION, MUTAGENESIS OF LYS-43 AND LYS-459.
    Category: Pathology & Biotech, PTM / Processing.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 11 other entries.

  13. 13
    "Eya1 and Eya2 proteins are required for hypaxial somitic myogenesis in the mouse embryo."
    Grifone R., Demignon J., Giordani J., Niro C., Souil E., Bertin F., Laclef C., Xu P.X., Maire P.
    Dev. Biol. 302:602-616(2007) [PubMed] [Europe PMC] [Abstract]
    Cited for: DISRUPTION PHENOTYPE, FUNCTION.
    Category: Function, Pathology & Biotech.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 30 other entries.

  14. 14
    "Tyrosine dephosphorylation of H2AX modulates apoptosis and survival decisions."
    Cook P.J., Ju B.G., Telese F., Wang X., Glass C.K., Rosenfeld M.G.
    Nature 458:591-596(2009) [PubMed] [Europe PMC] [Abstract]
    Cited for: DISRUPTION PHENOTYPE, FUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH H2AX.
    Category: Function, Subcellular Location, Pathology & Biotech, Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 5 and mapped to 29 other entries.

  15. 15
    "Regulation of mouse lens fiber cell development and differentiation by the Maf gene."
    Ring B.Z., Cordes S.P., Overbeek P.A., Barsh G.S.
    Development 127:307-317(2000) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:109344.

    This publication is mapped to 63 other entries.

  16. 16
    "Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development."
    Nishinakamura R., Matsumoto Y., Nakao K., Nakamura K., Sato A., Copeland N.G., Gilbert D.J., Jenkins N.A., Scully S., Lacey D.L., Katsuki M., Asashima M., Yokota T.
    Development 128:3105-3115(2001) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:109344.

    This publication is mapped to 45 other entries.

  17. 17
    "Misexpression of the eyes absent family triggers the apoptotic program."
    Clark S.W., Fee B.E., Cleveland J.L.
    J. Biol. Chem. 277:3560-3567(2002) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:109344.

    This publication is mapped to 29 other entries.

  18. 18
    "Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome."
    Buller C., Xu X., Marquis V., Schwanke R., Xu P.X.
    Hum. Mol. Genet. 10:2775-2781(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: MGI:109344, IntAct:P97767.

    This publication is mapped to 12 other entries.

  19. 19
    "Dach1, a vertebrate homologue of Drosophila dachshund, is expressed in the developing eye and ear of both chick and mouse and is regulated independently of Pax and Eya genes."
    Heanue T.A., Davis R.J., Rowitch D.H., Kispert A., McMahon A.P., Mardon G., Tabin C.J.
    Mech. Dev. 111:75-87(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Eya1 IS required for normal ear develoPMENTImported.
    Source: MGI:109344, GeneRIF:14048.

    This publication is mapped to 27 other entries.

  20. 20
    "Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six, Dach, and G proteins."
    Ozaki H., Watanabe Y., Ikeda K., Kawakami K.
    J. Hum. Genet. 47:107-116(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Impaired interactions between mouse Eyal harboring mutations found in patients with branchio-oto-renal syndrome and Six Dach and G proteinsImported.
    Source: GeneRIF:14048.

    This publication is mapped to 12 other entries.

  21. 21
    "Hox11 paralogous genes are essential for metanephric kidney induction."
    Wellik D.M., Hawkes P.J., Capecchi M.R.
    Genes Dev. 16:1423-1432(2002) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:109344.

    This publication is mapped to 29 other entries.

  22. 22
    "Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid."
    Xu P.X., Zheng W., Laclef C., Maire P., Maas R.L., Peters H., Xu X.
    Development 129:3033-3044(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Eya1 is required for the morphogenesis of mouse thymus parathyroid and thyroid.Imported.
    Source: MGI:109344, GeneRIF:14048.

    This publication is mapped to 47 other entries.

  23. 23
    "Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype."
    Goudreau G., Petrou P., Reneker L.W., Graw J., Loster J., Gruss P.
    Proc. Natl. Acad. Sci. U.S.A. 99:8719-8724(2002) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:109344.

    This publication is mapped to 103 other entries.

  24. 24
    "Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs."
    Okazaki Y., Furuno M., Kasukawa T., Adachi J., Bono H., Kondo S., Nikaido I., Osato N., Saito R., Suzuki H., Yamanaka I., Kiyosawa H., Yagi K., Tomaru Y., Hasegawa Y., Nogami A., Schonbach C., Gojobori T.
    , Baldarelli R., Hill D.P., Bult C., Hume D.A., Quackenbush J., Schriml L.M., Kanapin A., Matsuda H., Batalov S., Beisel K.W., Blake J.A., Bradt D., Brusic V., Chothia C., Corbani L.E., Cousins S., Dalla E., Dragani T.A., Fletcher C.F., Forrest A., Frazer K.S., Gaasterland T., Gariboldi M., Gissi C., Godzik A., Gough J., Grimmond S., Gustincich S., Hirokawa N., Jackson I.J., Jarvis E.D., Kanai A., Kawaji H., Kawasawa Y., Kedzierski R.M., King B.L., Konagaya A., Kurochkin I.V., Lee Y., Lenhard B., Lyons P.A., Maglott D.R., Maltais L., Marchionni L., McKenzie L., Miki H., Nagashima T., Numata K., Okido T., Pavan W.J., Pertea G., Pesole G., Petrovsky N., Pillai R., Pontius J.U., Qi D., Ramachandran S., Ravasi T., Reed J.C., Reed D.J., Reid J., Ring B.Z., Ringwald M., Sandelin A., Schneider C., Semple C.A., Setou M., Shimada K., Sultana R., Takenaka Y., Taylor M.S., Teasdale R.D., Tomita M., Verardo R., Wagner L., Wahlestedt C., Wang Y., Watanabe Y., Wells C., Wilming L.G., Wynshaw-Boris A., Yanagisawa M., Yang I., Yang L., Yuan Z., Zavolan M., Zhu Y., Zimmer A., Carninci P., Hayatsu N., Hirozane-Kishikawa T., Konno H., Nakamura M., Sakazume N., Sato K., Shiraki T., Waki K., Kawai J., Aizawa K., Arakawa T., Fukuda S., Hara A., Hashizume W., Imotani K., Ishii Y., Itoh M., Kagawa I., Miyazaki A., Sakai K., Sasaki D., Shibata K., Shinagawa A., Yasunishi A., Yoshino M., Waterston R., Lander E.S., Rogers J., Birney E., Hayashizaki Y.
    Nature 420:563-573(2002) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:109344.

    This publication is cited by 17060 and mapped to 39083 other entries.

  25. 25
    "Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice."
    Hulander M., Kiernan A.E., Blomqvist S.R., Carlsson P., Samuelsson E.-J., Johansson B.R., Steel K.P., Enerbaeck S.
    Development 130:2013-2025(2003) [PubMed] [Europe PMC] [Abstract]
    Source: MGI:109344.

    This publication is mapped to 37 other entries.

1 to 25 of 132  Show